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Iron-Catalyzed C–H/N–H Activations for Annulation of Allenes, Alkynes, and Bicyclopropylidenes

dc.contributor.advisorAckermann, Lutz Prof. Dr.
dc.contributor.authorMo, Jiayu
dc.date.accessioned2020-11-16T14:00:46Z
dc.date.available2020-11-16T14:00:46Z
dc.date.issued2020-11-16
dc.identifier.urihttp://hdl.handle.net/21.11130/00-1735-0000-0005-14F0-5
dc.identifier.urihttp://dx.doi.org/10.53846/goediss-8299
dc.language.isoengde
dc.publisherNiedersächsische Staats- und Universitätsbibliothek Göttingende
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.ddc540de
dc.titleIron-Catalyzed C–H/N–H Activations for Annulation of Allenes, Alkynes, and Bicyclopropylidenesde
dc.typedoctoralThesisde
dc.contributor.refereeAckermann, Lutz Prof. Dr.
dc.date.examination2020-10-26
dc.description.abstractengIron-catalyzed C–H/N–H activations for the annulation of allenes, alkynes, and bicyclopropylidenes were realized by using a customizable clickable triazole amide under mild reaction conditions. The powerful iron catalysis occurred under external‐oxidant‐free conditions even at room temperature. A unifying mechanistic approach combining experiments, Mössbauer spectroscopy was employed to delineate the reaction mechanisms. The synthetic utility of the iron‐catalyzed oxidant‐free C−H functionalizations was illustrated by the traceless removal of the modular TAH/TAM group in a user‐friendly fashion.de
dc.contributor.coRefereeBreder, Alexander Dr.
dc.contributor.thirdRefereeTietze, Lutz Prof. Dr. Dr.
dc.contributor.thirdRefereeBennati, Marina Prof. Dr.
dc.contributor.thirdRefereeMata, Ricardo Prof. Dr.
dc.contributor.thirdRefereeWalker, Johannes Jun.-prof. Dr.
dc.subject.engIronde
dc.subject.engC–H Activationde
dc.subject.engAllenesde
dc.subject.engBicyclopropylidenesde
dc.subject.engalkynesde
dc.subject.engredox-neutral reactionsde
dc.identifier.urnurn:nbn:de:gbv:7-21.11130/00-1735-0000-0005-14F0-5-4
dc.affiliation.instituteFakultät für Chemiede
dc.subject.gokfullChemie  (PPN62138352X)de
dc.identifier.ppn1738860612


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